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低剂量甲氨蝶呤治疗成人斯蒂尔病的糖皮质激素节省效应。

Corticosteroid sparing effect of low dose methotrexate treatment in adult Still's disease.

作者信息

Fautrel B, Borget C, Rozenberg S, Meyer O, Le Loët X, Masson C, Koeger A C, Kahn M F, Bourgeois P

机构信息

Department of Rheumatology, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

出版信息

J Rheumatol. 1999 Feb;26(2):373-8.

PMID:9972972
Abstract

OBJECTIVE

Adult Still's disease (ASD) is a rare chronic polyarthritis, usually treated with corticosteroid therapy. Because some patients become dependent on high dose prednisone or are refractory to that treatment, and because adverse events are frequent with corticosteroid, we evaluated the efficacy of low dose methotrexate (MTX) as a second-line drug.

METHODS

We retrospectively studied 26 patients with ASD treated with low dose MTX because their disease was either resistant to or dependent on corticosteroids.

RESULTS

The group included 13 women and 13 men, with a mean age of 32.6 years at onset of ASD. Mean disease duration at the beginning of MTX treatment was 59.9 mo (range 7 to 444). Evaluation took place at the maximum followup, which averaged 48.9 mo (range 8 to 136). The mean dose of MTX was 11.5+/-3.6 mg/week (range 7.5 to 17.5). Twenty-three patients responded to MTX; 18 had complete remission. No difference was seen between patients with or without extraarticular manifestations. Leukocyte and neutrophil counts and erythrocyte sedimentation rate were significantly reduced (p = 0.0001). Daily prednisone intake decreased by 69% (21.5 mg) (p = 0.0001). Eleven patients were able to stop taking corticosteroids. One patient with AA amyloidosis renal failure died of neutropenia: this was the only serious adverse event.

CONCLUSION

MTX is an effective second-line treatment of ASD that does not respond to prednisone. It allows significant reduction of corticosteroid doses, which is beneficial to these patients, who have frequent and numerous corticosteroid related adverse events.

摘要

目的

成人斯蒂尔病(ASD)是一种罕见的慢性多关节炎,通常采用皮质类固醇疗法进行治疗。由于一些患者会对高剂量泼尼松产生依赖或对该治疗无效,且皮质类固醇治疗频繁出现不良事件,我们评估了低剂量甲氨蝶呤(MTX)作为二线药物的疗效。

方法

我们回顾性研究了26例接受低剂量MTX治疗的ASD患者,这些患者的疾病对皮质类固醇耐药或依赖。

结果

该组包括13名女性和13名男性,ASD发病时的平均年龄为32.6岁。MTX治疗开始时的平均病程为59.9个月(范围7至444个月)。在最长随访时进行评估,平均随访时间为48.9个月(范围8至136个月)。MTX的平均剂量为11.5±3.6毫克/周(范围7.5至17.5毫克/周)。23例患者对MTX有反应;18例完全缓解。有或无关节外表现的患者之间未见差异。白细胞、中性粒细胞计数和红细胞沉降率显著降低(p = 0.0001)。每日泼尼松摄入量减少了69%(21.5毫克)(p = 0.0001)。11例患者能够停用皮质类固醇。1例患有AA淀粉样变性肾衰竭的患者死于中性粒细胞减少症:这是唯一的严重不良事件。

结论

MTX是对泼尼松无反应的ASD的有效二线治疗药物。它能显著降低皮质类固醇剂量,这对这些频繁出现大量与皮质类固醇相关不良事件的患者有益。

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